Search Results - "Delgado Pecellín, Isabel"
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False negatives in the newborn screening for cystic fibrosis in Western Andalusia: Results from a 10‐year experience
Published in Pediatric pulmonology (01-09-2023)“…Cystic fibrosis (CF) is the most common autosomal recessive disorder in the Caucasian population, with an incidence of 1:5000 live births. In 2011, the…”
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Severe Anemia in Infants: Don’t Miss the Clues
Published in Clinical pediatrics (01-11-2023)Get full text
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Evaluation of bone metabolism in children with cystic fibrosis
Published in Bone (New York, N.Y.) (01-06-2021)“…Cystic fibrosis (CF) bone disease (CFBD) has attracted considerable recent interest from researchers, although several aspects of CFBD pathophysiology remain…”
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Experience With Elexacaftor/Tezacaftor/Ivacaftor in Patients With Cystic Fibrosis and Advanced Disease
Published in Archivos de bronconeumología (English ed.) (01-09-2023)“…[Display omitted] Elexacaftor/tezacaftor/ivacaftor (ETI) was used through the early access programme in Spain from December 2019 in cystic fibrosis (CF)…”
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Lung Growth and Aging: A Complex and Increasingly Confounding Network
Published in Archivos de bronconeumología (English ed.) (01-09-2019)Get full text
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Results of the Andalusian Cystic Fibrosis Neonatal Screening Program, 5 Years After Implementation
Published in Archivos de bronconeumología (English ed.) (01-11-2018)“…INTRODUCTIONCystic fibrosis neonatal screening (CFNS), based on double determination of immunoreactive trypsinogen ([IRT] [IRT1/IRT2]), has been available in…”
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Compassionate Use of Lumacaftor/Ivacaftor in Cystic Fibrosis: Spanish Experience
Published in Archivos de bronconeumología (English ed.) (01-12-2018)“…Graphical abstract…”
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Spanish multicentre study on morbidity and pathogenicity of tracheal bronchus in children
Published in Pediatric pulmonology (01-10-2019)“…Tracheal bronchus (TRB) has been generally considered an anatomical variant of the tracheobronchial tree without a precise pathological effect. Its prevalence…”
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Mortality from cystic fibrosis in Europe: 1994-2010
Published in Pediatric pulmonology (01-02-2016)“…Summary Objective To date, available mortality trends due to cystic fibrosis (CF) have been limited to the analysis of certain countries in different parts of…”
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CFTR protein repair therapy in cystic fibrosis
Published in Archivos de bronconeumología (English ed.) (01-04-2014)“…Cystic fibrosis is a single gene, autosomal recessive disorder, in which more than 1,900 mutations grouped into 6 classes have been described. It is an example…”
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Management of postintubation tracheal rupture in pediatric patients
Published in Archivos de bronconeumología (01-05-2009)Get full text
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Pulmonary function and bronchopulmonary dysplasia classification: insights from the Spanish Registry
Published in European journal of pediatrics (01-09-2024)“…In 2016, the Spanish Research Group on Bronchopulmonary Dysplasia (BPD) (GEIDIS) established a national registry with participation of 66 hospitals to collect…”
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Mycobacterium lentiflavum in Cystic Fibrosis Subjects. A Colonizer or a True Pathogen?
Published in Archivos de bronconeumología (English ed.) (01-12-2018)Get full text
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Primary Endobronchial Tumors in Childhood
Published in Archivos de bronconeumología (English ed.) (01-11-2018)Get full text
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Lung Growth and Aging: A Complex and Increasingly Confounding Network
Published in Archivos de bronconeumología (English ed.) (01-09-2019)Get full text
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CFTR Protein Repair Therapy in Cystic Fibrosis
Published in Archivos de bronconeumología (English ed.) (01-04-2014)“…Abstract Cystic fibrosis is a single gene, autosomal recessive disorder, in which more than 1900 mutations grouped into 6 classes have been described. It is an…”
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Fiberoptic Bronchoscopy Findings in Children With Stridor in a Tertiary Hospital
Published in Archivos de bronconeumología (English ed.) (01-06-2016)Get full text
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Fiberoptic bronchoscopy findings in children with stridor in a tertiary hospital
Published in Archivos de bronconeumología (English ed.) (01-06-2016)Get full text
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Compassionate Use of Lumacaftor/Ivacaftor in Cystic Fibrosis: Spanish Experience
Published in Archivos de bronconeumología (English ed.) (01-12-2018)“…[Display omitted] The most common cystic fibrosis (CF)-causing mutation is deltaF508 (F508del), which is present in 28% of CF Spanish patients. While the…”
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